Positions

Selected Publications

Academic Article

Year Title Altmetric
2019 Analytical Methods for Quantitative Plasma Carnitine Determination 2019
2018 Laboratory analysis of amino acids, 2018 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG) 2018
2018 Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency 2018
2017 Association of acute toxic encephalopathy with litchi consumption in an outbreak in Muzaffarpur, India, 2014: a case-control study 2017
2017 Methods for quantitative creatinine determination 2017
2017 Laboratory diagnosis of creatine deficiency syndromes: A technical standard and guideline of the American College of Medical Genetics and Genomics 2017
2016 An overview of biochemical genetics 2016
2016 Quantitative analysis of total plasma homocysteine by LC-MS/MS 2016
2014 Carnitine Palmitoyltransferase 1b Deficiency Protects Mice from Diet-Induced Insulin Resistance. 2014
2014 Carnitine Palmitoyltransferase 1b Deficient Mice Develop Severe Insulin Resistance After Prolonged High Fat Diet Feeding. 2014
2014 Comparison of Methods, Storage Conditions, and Time to Analysis of Serum and Urine Creatinine Measured from Microsamples by Liquid Chromatography Mass Spectrometery (LC/MS) vs. Jaffe 2014
2013 Simultaneous quantification of F2-isoprostanes and prostaglandins in human urine by liquid chromatography tandem-mass spectrometry 2013
2012 The development and implementation of an in-service exam for medical genetics residency programs 2012
2012 Biochemical genetics. Introduction. 2012
2012 Teaching mitochondrial genetics & disease: A GENA project curriculum intervention 2012
2011 Mitochondrial genetics. 2011
2011 An overview of biochemical genetics 2011
2010 Biochemical genetics 2010
2009 Mitochondrial genetics 2009
2008 Biochemical genetics 2008
2008 Homozygous carnitine palmitoyltransferase 1b (muscle isoform) deficiency is lethal in the mouse 2008
2005 The adenine nucleotide translocase type 1 (ANT1): A new factor in mitochondrial disease 2005
2005 Medium-chain acyl-CoA dehydrogenase deficiency in gene-targeted mice. 2005
2005 An overview of biochemical genetics. 2005
2005 Assays used in the analysis of Arl2 and its binding partners 2005
2003 Cytosolic Arl2 Is Complexed with Cofactor D and Protein Phosphatase 2A 2003
2002 ARL2 and BART enter mitochondria and bind the adenine nucleotide transporter 2002
2001 ADP-ribosylation factors (ARFs) and ARF-like 1 (ARL1) have both specific and shared effectors. Characterizing ARL1-binding proteins 2001
1999 The function of conserved amino acid residues adjacent to the effector domain in elongation factor G 1999
1999 The ARF-like 2 (ARL2)-binding protein, BART. Purification, cloning, and initial characterization 1999
1995 Cross-species complementation of the indispensable Escherichia coli era gene highlights amino acid regions essential for activity 1995
1994 GTPase-dependent signaling in bacteria: Characterization of a membrane- binding site for Era in Escherichia coli 1994
1994 In vivo selection of conditional-lethal mutations in the gene encoding elongation factor G of Escherichia coli 1994

Chapter

Year Title Altmetric
2014 Amino Acid Disorders.  1-788. 2014
2014 Amino Acid Disorders.  136-147. 2014
2010 Mechanisms of Toxicity in Fatty Acid Oxidation Disorders.  317-348. 2010

Education And Training

  • Emory University School of Medicine Pediatrics/Human Genetics, Postdoctoral Fellowship 2004
  • Emory University School of Medicine Biochemistry, Postdoctoral Fellowship 2001
  • National Cancer Institute Biochemistry, Postdoctoral Fellowship 1996
  • Full Name

  • Jon Sharer